Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06605469

Ejaculatory and Orgasmic Dysfunction Registry (Climax Registry)

Led by Charitable Union for the Research and Education of Peyronie's Disease · Updated on 2025-02-14

500

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting an observational study to create a large national registry that evaluates the safety and effectiveness of treatments for men experiencing ejaculatory and/or orgasmic dysfunctions. The study aims to capture important outcomes from men receiving therapy for these conditions to better understand treatment results. This collaboration with the Sexual Medicine Society of North America helps inform sexual medicine providers and encourage patient participation. Participants, including men receiving treatment and their sexual partners, will be invited by their local providers to join the study. They will complete questionnaires about their diagnosis and treatment effectiveness at the start of the study, then every three months for one year, followed by every six months for two additional years. Patient partners may also enroll and follow the same questionnaire schedule. During the study, participants will provide information through regular questionnaires over a three-year period. Researchers will use these responses to assess primary outcomes related to treatment safety and efficacy. This ongoing data collection will help build a comprehensive understanding of therapies for ejaculatory and orgasmic dysfunctions and contribute to future care improvements.

CONDITIONS

Brief Title

Ejaculatory and Orgasmic Dysfunction Registry

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Men being treated for either ejaculatory and/or orgasmic dysfunction
  • Sexual partners of men receiving treatment for ejaculatory and/or orgasmic dysfunction
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote)

Surveillance

Duration - 3 years

Participants complete questionnaires about ejaculatory and orgasmic function at baseline and periodically over time to monitor outcomes.

1 baseline questionnaire, then questionnaires every 3 months for 1 year, followed by every 6 months for 2 years

Trial Site Locations

Total: 1 location

1

The Male Fertility and Peyronie's Clinic

Orem, Utah, United States, 84057

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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